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Names | |||
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Preferred IUPAC name
6-Diazo-2,4-dinitrocyclohexa-2,4-dien-1-one | |||
Identifiers | |||
3D model (JSmol)
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Abbreviations | DDNP | ||
ChemSpider | |||
ECHA InfoCard | 100.022.849 | ||
EC Number |
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PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C6H2N4O5 | |||
Molar mass | 210.105 g·mol−1 | ||
Insoluble | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Diazodinitrophenol (DDNP) was the first diazo compound produced; it was subsequently used to make dyes and explosives. It forms yellow crystals in pure form; however, the color of impure forms may vary from dark yellow to green to dark brown.[1] It is soluble in acetic acid, acetone, concentrated hydrochloric acid, like most non-polar solvents and is slightly soluble in water.[2]
A solution of cold sodium hydroxide may be used to destroy it.[3] DDNP may be desensitized by immersing it in water, as it does not react in water at normal temperature. It is less sensitive to impact but more powerful than mercury fulminate and almost as powerful as lead azide.[4] The sensitivity of DDNP to friction is much less than that of mercury fulminate and lead azide.
DDNP is used with other materials to form priming mixtures, particularly where a high sensitivity to flame or heat is desired. DDNP is often used as an initiating explosive in propellant primer devices and is a substitute for lead styphnate in what are termed "green" or "non-toxic" (lead free) priming explosive compositions. Lead free primers have been judged as inadequate for service use in firearms due to weak and uneven initiation compared to lead based primers.[5]